Boc-His(Trt)-OH: Your Key Building Block for Advanced Peptide Synthesis and Research

Unlock new possibilities in peptide synthesis with our high-quality Boc-His(Trt)-OH.

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Key Advantages for Your Research

Suppressed Racemization

Utilize the Trityl group on histidine's imidazole side chain to significantly reduce racemization, ensuring the stereochemical integrity of your synthesized peptides and crucial for precise peptide drug development.

Enhanced Peptide Stability

The inclusion of Aib, an unnatural amino acid, promotes helical structures, thereby increasing peptide resistance to enzymatic degradation and extending its half-life, which is vital for peptide synthesis building blocks.

Seamless Boc Chemistry Integration

Benefit from the compatibility of Boc and Trt groups, which are cleaved under similar acidic conditions (TFA), simplifying deprotection steps and streamlining your solid phase peptide synthesis workflow.

Key Applications

Peptide Drug Development

Essential for creating peptides targeting diseases, where the stability and specific conformations enabled by Boc-His(Trt)-OH are crucial for effective therapeutics.

Biomedical Research

A valuable tool for studying peptide interactions, designing enzyme mimics, and exploring structure-activity relationships in various biological systems.

Custom Peptide Synthesis

Enables researchers to design and synthesize custom peptides with unique sequences and properties, supporting diverse research goals.

DNA-Encoded Libraries

Supports the rapid exploration of peptide chemical space for drug discovery by facilitating synthesis compatible with library generation techniques.